Canonical Allele Identifier: CA1819427316
Gene: CCDC26 HGNC NCBI

Linked Data

dbSNP Id: rs1661561612

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.129633441C>A , CM000670.2:g.129633441C>A GRCh38
NC_000008.10:g.130645687C>A , CM000670.1:g.130645687C>A GRCh37
NC_000008.9:g.130714869C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_130917.1:n.312+46487G>T